Variant report

Variant	rs11591853
Chromosome Location	chr10:117496314-117496315
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs11598238	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12766958	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12767442	0.88[AFR][1000 genomes]
rs2532696	0.82[AFR][1000 genomes]
rs2532697	0.82[AFR][1000 genomes]
rs2532698	0.80[AFR][1000 genomes]
rs2532700	0.82[AFR][1000 genomes]
rs2532702	0.82[AFR][1000 genomes]
rs2532703	0.82[AFR][1000 genomes]
rs2532710	0.83[AFR][1000 genomes]
rs2532711	0.90[AFR][1000 genomes]
rs2532715	0.87[AFR][1000 genomes]
rs2804167	0.90[AFR][1000 genomes]
rs2804168	0.90[AFR][1000 genomes]
rs2804169	0.90[AFR][1000 genomes]
rs2804170	0.83[AFR][1000 genomes]
rs2804171	0.84[AFR][1000 genomes]
rs2804172	0.82[AFR][1000 genomes]
rs2907524	0.86[AFR][1000 genomes]
rs2907527	0.82[AFR][1000 genomes]
rs2907528	0.82[AFR][1000 genomes]
rs2907530	0.82[AFR][1000 genomes]
rs2907532	0.82[AFR][1000 genomes]
rs2907533	0.82[AFR][1000 genomes]
rs2907534	0.82[AFR][1000 genomes]
rs2907535	0.82[AFR][1000 genomes]
rs2907536	0.82[AFR][1000 genomes]
rs2907538	0.82[AFR][1000 genomes]
rs2907539	0.82[AFR][1000 genomes]
rs2907540	0.82[AFR][1000 genomes]
rs2907541	0.82[AFR][1000 genomes]
rs2907542	0.82[AFR][1000 genomes]
rs2960636	0.82[AFR][1000 genomes]
rs2960637	0.82[AFR][1000 genomes]
rs2960638	0.82[AFR][1000 genomes]
rs2960639	0.82[AFR][1000 genomes]
rs2960642	0.84[AFR][1000 genomes]
rs2960643	0.82[AFR][1000 genomes]
rs2960644	0.82[AFR][1000 genomes]
rs2960646	0.82[AFR][1000 genomes]
rs2960647	0.82[AFR][1000 genomes]
rs2960648	0.82[AFR][1000 genomes]
rs2960649	0.82[AFR][1000 genomes]
rs2960652	0.82[AFR][1000 genomes]
rs2960654	0.90[AFR][1000 genomes]
rs2960731	0.81[AFR][1000 genomes]

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117489400-117520800	Weak transcription	HSMM	muscle
2	chr10:117490800-117509600	Weak transcription	Aorta	Aorta
3	chr10:117496000-117496800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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